INTERNATIONAL FOXP1 FOUNDATION

Functional restoration of foxp1 haploinsufficiency using aav-mediated gene rescue in the brain-understanding foxp1 function in the mouse brain is crucial to develop effective therapeutics for foxp1 syndrome in humans. In this project, we will use a mouse model that mimics the genetic basis of many forms of foxp1 syndrome, where only one out of the two functional copies of foxp1 gene is present. We will perform intracerebroventricular (icv) injections of a unique adeno associated virus (aav) called aav9 and/or its modified and improvised version (aav-php.eb) at an early developmental stage to restore foxp1 expression in the brains of these mice. In this strategy, foxp1 will be re-expressed under the control of the human synapsin 1 promoter, ensuring neuron specific expression. We will then examine whether foxp1 gene replacement can correct behavioral deficits in the mice. If successful, we will extend the gene restoration to later developmental time points to determine a potential critical window of gene replacement therapy in this mouse model. Results from this project should provide fundamental knowledge about the feasibility of foxp1 gene therapy in humans and form the basis for future clinical trials.